Water transport in maize roots under the influence of mercuric chloride and water stress: A role of water channels

Biologia Plantarum

Volumn 50, Issue 1, 2006, Pages 74-80

  Ionenko, I F ^a   Anisimov, A V ^a   Karimova, F G ^a  

^a KAZAN INSTITUTE OF BIOCHEMISTRY AND BIOPHYSICS   (Russian Federation)

Author keywords

Diffusion rate; Nuclear magnetic resonance; Transmembrane transfer; Zea mays

Indexed keywords

ZEA MAYS;

EID: 28444439576     PISSN: 00063134     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10535-005-0077-7     Document Type: Article

References (47)

1. Abraham, A.: The Principles of Nuclear Magnetism. - Oxford University Press, London 1961.
2. Anisimov, A.V., Evarestov, A.S., Ionenko, I.F., Gusev, N.A.: [Pulsed NMR method for estimation of intercellular water transport on symplasm.] - Dokl. Akad. Nauk SSSR 271: 1246-1249, 1983. [In Russ.]
3. Anisimov, A.V., Ratković, S.: Transport Vody v Rasteniyakh: Issledovanie Impul'snym Metodom YaMR. [Water Transport in Plants: Determination by pulsed NMR.] - Nauka, Moskva 1992. [In Russ.]
4. Anisimov, A.V., Sorokina, N.Yu., Dautova, N.R.: Water diffusion in biological porous systems: a NMR approach. - Magn. Resonance Imaging 16: 565-568, 1998.
5. 2 on water transport across root cells of maize (Zea mays L.) seedlings. - Plant Physiol. 99: 886-894, 1992.
6. Baiges, I., Schäffner, A.R., Affenzeller, M.J., Mas, A.: Plant aquaporins. - Physiol. Plant. 115: 175-182, 2002.
7. Barrieu, F., Chaumont, F., Chrispeels, M.J.: High expression of the tonoplast aquaporin ZmTIP1 in epidermal and conducting tissues of maize. - Plant Physiol. 117: 1153-1163, 1998.
8. Barrowclough, D.E., Peterson, C.A., Steudle, E.: Radial hydraulic conductivity along developing onion roots. - J. exp. Bot. 51: 547-557, 2000.
9. Carvajal, M., Cooke, D.T., Clarkson, D.T.: Responses of wheat plants to nutrient deprivation may involve the regulation of water-channel function. - Planta 199: 372-381, 1996.
10. Carvajal, M., Martinez, V., Alcaraz, C.F.: Physiological function of water channels is affected by salinity in roots of paprika pepper. - Physiol. Plant. 105: 95-101, 1999.
11. Chaumont, F., Barrieu, F., Herman, E.M., Chrispeels, M.J.: Characterization of a maize tonoplast aquaporin expressed in zones of cell division and elongation. - Plant Physiol. 117: 1143-1152, 1998.
12. Chaumont, F., Barrieu, F., Wojcik, E., Chrispeels, M.J., Jung, R.: Aquaporins constitute a large and highly divergent protein family in maize. - Plant Physiol. 125: 1206-1215, 2001.
13. Chrispeels, M.J., Maurel, C.: Aquaporins: the molecular basis of facilitated water movement through living plant cells. - Plant Physiol. 105: 9-15, 1994.
14. Clarkson, D.T., Carvajal, M., Henzler, T., Waterhouse, R.N., Smyth, A.J., Cooke, D.T., Steudle, E.: Root hydraulic conductance: diurnal aquaporin expression and the effects of nutrient stress. - J. exp. Bot. 51: 61-70, 2000.
15. Cooper, R.L., Chang, D.B., Young, A.C., Martin, C.J., Ancker-Johnson, B.: Restricted diffusion in biological systems. - Biophys.J. 14: 161-177, 1974.
16. Crick, F.: Diffusion in embryogenesis. - Nature 225: 420-422, 1970.
17. Farrar, T.C., Becker, E.D.: Pulse and Fourier Transform NMR. - Academic Press, New York 1971.
18. Frensch, J., Hsiao, T.S.: Transient responses of cell turgor and growth of maize roots as affected by changes in water potential. - Plant Physiol. 104: 247-254, 1994.
19. Guerrero, F.D., Jones, J.T., Mullet, J.E.: Turgor-responsive gene transcription and RNA levels increase rapidly when pea shoots are wilted. Sequence and expression of three inducible genes. - Plant mol. Biol. 15: 11-26, 1990.
20. Henzler, T., Steudle, E.: Reversible closing of water channels in Chara internodes provides evidence for a composite transport model of the plasma membrane. - J. exp. Bot. 46: 199-209, 1995.
21. Hukin, D., Doering-Saad, C., Thomas, C.R., Pritchard, J.: Sensitivity of cell hydraulic conductivity to mercury is coincident with symplasmic isolation and expression of plasmalemma aquaporin genes in growing maize roots. - Planta 215: 1047-1056, 2002.
22. Ionenko, I.F., Anisimov, A.V.: Effect of water deficit and membrane destruction on water diffusion in the tissues of maize seedlings. - Biol. Plant. 44: 247-252, 2001.
23. Javot, H., Maurel, C.: The role of aquaporins in root water uptake. - Ann. Bot. 90: 301-313, 2002.
24. Johansson, I., Karlsson, M., Shukla, V.K., Chrispeels, M.J., Larsson, C., Kjellbom, P.: Water transport activity of plasma membrane aquaporin PM28A is regulated by phosphorylation. - Plant Cell 10: 451-459, 1998.
25. 2+ and apoplastic water potential. - Plant Cell 8: 1181-1191, 1996.
26. Kaldenhoff, R., Grote, K., Zhu, J.-J., Zimmermann, U.: Significance of plasmalemma aquaporins for water-transport in Arabidopsis thaliana. - Plant J. 14: 121-128, 1998.
27. Kjellbom, P., Larsson, C., Johansson, I., Karisson, M., Johanson, U.: Aquaporins and water homeostasis in plants. - Trends Plant Sci. 4: 308-314, 1999.
28. Krishnan, P., Joshi, D.K., Maheswari, M., Nagarajan, S., Moharir, A.V.: Characterization of soybean and wheat seeds by nuclear magnetic resonance spectroscopy. - Biol. Plant. 48: 117-120, 2004.
29. Kuzmanoff, K.M., Evans, M.L.: Kinetics of adaptation to osmotic stress in lentil (Lens culinaris Med.) roots. - Plant Physiol. 68: 244-247, 1981.
30. Maggio, A., Joly, R.J.: Effects of mercuric chloride on the hydraulic conductivity of tomato root systems. - Plant Physiol. 109: 331-335, 1995.
31. Maurel, C., Kado, R.T., Guern, J., Chrispeels, M.J.: Phosphorylation regulates the water channel activity of the seed specific aquaporin α-TIP. - EMBO J. 14: 3028-3035, 1995.
32. Murata, K., Mitsuoka, K., Hirai, T., Walz, T., Agre, P., Heymann, J.B., Engel, A., Fijlyoshi, Y.: Structural determinants of water permeation through aquaporin 1. - Nature 107: 599-605, 2000.
33. Snaar, J.E.M., Van As, H.: Probing water compartment and membrane permeability in plant cells by proton NMR relaxation measurements. - Biophys. J. 63: 1654-1658, 1992.
34. Stejskal, E.O., Tanner, J.E.: Spin-diffusion measurements: spin-echoes in the presence of a time-dependent field gradient. - J. chem. Phys. 42: 288-292, 1965.
35. Steudle, E.: Water transport across plant tissue: role of water channels. - Biol. Cell 89: 259-273, 1997.
36. Steudle, E.: Water uptake by roots: effect of water deficit. - J. exp. Bot. 51: 1531-1542, 2000.
37. Tanner, J.E.: Use of the stimulated echo in NMR diffusion studies. - J. chem. Phys. 52: 2523-2526, 1970.
38. Tazawa, M., Ohkuma, E., Shibasaka, M., Nakashima, S.: Mercurial-sensitive water transport in barley roots. - J. Plant Res. 110: 435-442, 1997.
39. Tyerman, S.D., Bohnert, H.J., Maurel, S., Steudle, E., Smith, J.A.C.: Plant aquaporins: their molecular biology, biophysics and significance for plant water relations. - J. exp. Bot. 50: 1055-1071, 1999.
40. 1H spin-echo nuclear magnetic resonance in plant tissue. The effect of Mn (II) and water content in wheat leaves. - Biophys. J. 32: 1043-1051, 1980.
41. Van Dusschoten, D., De Jager, P.A., Van As, H.: Extracting diffusion constants from echo-time-dependent PFG NMR data using relaxation-time information. - J. Magn. Resonance 116: 22-28, 1995.
42. Van der Weerd, L., Claessens, M.M.A.E., Rutink, T., Vergeldt, F.J., Schaafsma, T.J., Van As, H.: Quantitative NMR microscopy of osmotic stress responses in maize and pearl millet. - J. exp. Bot. 52: 2333-2343, 2001.
43. Wan, X., Zwiazek, J.J.: Mercuric chloride effects on root water transport in aspen seedlings. - Plant Physiol. 121: 939-946, 1999.
44. Willmer, C.M., Padmasree, K., Raghavendra, A.S.: A novel method of measuring volume changes of mesophyll cell protoplasts and the effect of mercuric chloride on their osmotically-induced swelling. - J. exp. Bot. 50: 401-406, 1999.
45. Yamada, S., Katsuhara, M., Kelly, W., Michalowski, C.B., Bohnert, H.J.: A family of transcripts encoding water channel proteins: tissue-specific expression in the common ice plant. - Plant Cell 7: 1129-1142, 1995.
46. Yamaguchi-Shinozaki, K., Koizumi, M., Urao, S., Shinozaki, K.: Molecular cloning and characterization of 9 cDNAs for genes that are responsive to desiccation in Arabidopsis thaliana: sequence analysis of qne cDNA clone that encodes a putative transmembrane channel protein. - Plant Cell Physiol. 33: 217-224, 1992.
47. 2 in intact wheat root cells. - Plant Physiol. 120: 849-858, 1999.